A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016918



Internal ID18759453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88950439..88982308hg38UCSC Ensembl
Innerchr7:88579753..88611622hg19UCSC Ensembl
Innerchr7:88417689..88449558hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3831870
hg1931870
hg1831870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655210, nssv3655209
Samples
Known GenesZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016918
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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