A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526330



Internal ID15106937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146645230..146674089hg38UCSC Ensembl
Innerchr7:146342322..146371181hg19UCSC Ensembl
Innerchr7:145973255..146002114hg18UCSC Ensembl
Innerchr7:145779970..145808829hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3828860
hg1928860
hg1828860
hg1728860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702620
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526330
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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