A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757753



Internal ID18709348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158725311..159162536hg38UCSC Ensembl
Innerchr7:158518002..158955227hg19UCSC Ensembl
Innerchr7:158210763..158647988hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38437226
hg19437226
hg18437226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033545
Supporting Variants
Samples
Known GenesESYT2, LINC00689, VIPR2, WDR60
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3757753
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer