A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022814



Internal ID19112032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16222675..16300363hg38UCSC Ensembl
Innerchr7:16262300..16339988hg19UCSC Ensembl
Innerchr7:16228825..16306513hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3877689
hg1977689
hg1877689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643195, nssv3643194
Samples
Known GenesISPD, ISPD-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022814
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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