A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156737



Internal ID22087138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143521875..143870966hg38UCSC Ensembl
Outerchr7:143521765..143875073hg38UCSC Ensembl
Innerchr7:143218968..143568059hg19UCSC Ensembl
Outerchr7:143218858..143572166hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38353309
hg19353309
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022468, nssv4022459, nssv4022482, nssv4022467, nssv4019585, nssv4022472, nssv4019582, nssv4022471, nssv4022463, nssv4022460, nssv4019586, nssv4022478, nssv4022474, nssv4022464, nssv4022466, nssv4019575, nssv4022457, nssv4022465, nssv4019579, nssv4022470, nssv4022483, nssv4022469, nssv4022476, nssv4022458, nssv4022477, nssv4022461, nssv4019577, nssv4019584, nssv4019578, nssv4019587, nssv4019576, nssv4022481, nssv4022480, nssv4019580, nssv4019581, nssv4019583, nssv4022485, nssv4022475, nssv4022479
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115A, FAM115C, LOC154761
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156737
Frequency
Sample Size131
Observed Gain30
Observed Loss9
Observed Complex0
Frequencyn/a


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