A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657880



Internal ID15394532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62575192..62590140hg38UCSC Ensembl
Innerchr7:62035570..62050518hg19UCSC Ensembl
Innerchr7:61673005..61687953hg18UCSC Ensembl
Innerchr7:61479720..61494668hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3814949
hg1914949
hg1814949
hg1714949
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516283
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657880
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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