A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133661



Internal ID19287157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:74981059..75064687hg38UCSC Ensembl
Outerchr7:74395200..74480500hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3883629
hg1985301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3593n106
Supporting Variantsnssv3969230
SamplesKWS2
Known GenesWBSCR16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133661
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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