A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969911



Internal ID22744846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16619297..16951954hg38UCSC Ensembl
chr1:16945792..17278449hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38332658
hg19332658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359444
Samples
Known GenesCROCC, CROCCP2, ESPNP, LOC729574, MIR3675, MST1L, MST1P2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969911
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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