A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656461



Internal ID18608056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72577915..72842566hg38UCSC Ensembl
Innerchr7:72042900..72313144hg19UCSC Ensembl
Innerchr7:71680836..71951080hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38264652
hg19270245
hg18270245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023444
Supporting Variants
Samples
Known GenesMIR4650-1, MIR4650-2, SBDSP1, TYW1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3656461
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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