A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021536



Internal ID19110754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56740406..56908389hg38UCSC Ensembl
Innerchr7:56808099..56976080hg19UCSC Ensembl
Innerchr7:56775593..56943574hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38167984
hg19167982
hg18167982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6364n100
Supporting Variantsnssv3661479
Samples
Known GenesLOC100130849
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021536
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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