A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3698903



Internal ID18650498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16636806..16721972hg38UCSC Ensembl
Innerchr1:16963301..17048467hg19UCSC Ensembl
Innerchr1:16835888..16921054hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3885167
hg1985167
hg1885167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003822
Supporting Variants
Samples
Known GenesESPNP, LOC729574, MIR3675, MST1P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3698903
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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