A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140861



Internal ID18934952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152405657..152405712hg38UCSC Ensembl
Outerchr7:152102742..152102797hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986775, nssv3992363
SamplesKWS1, KWS2
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140861
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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